莱施-奈恩综合征。临床特征总结。 - Suppr

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Lesch-Nyhan syndrome. Summary of clinical features.

作者信息

Nyhan W L

出版信息

Fed Proc. 1968 Jul-Aug;27(4):1034-41.

PMID:5658469

Abstract

摘要

相似文献

Lesch-Nyhan syndrome. Summary of clinical features.莱施-奈恩综合征。临床特征总结。

Fed Proc. 1968 Jul-Aug;27(4):1034-41.

Clinical features of the Lesch-Nyhan syndrome. Introduction--clinical and genetic features.莱施-奈恩综合征的临床特征。引言——临床和遗传特征。

Fed Proc. 1968 Jul-Aug;27(4):1027-33.

Clinical features of the Lesch-Nyhan syndrome.莱施-奈恩综合征的临床特征。

Arch Intern Med. 1972 Aug;130(2):186-92.

[Self mutilation of the lower lip, associated with athetosis and oligophrenia without purine metabolism disorder ("pseudo Lesch-Nyhan syndrome")].[下唇自残，伴手足徐动症和智力发育迟缓，无嘌呤代谢紊乱（“假性莱施-奈恩综合征”）]

Hautarzt. 1973 Apr;24(4):158-60.

The urinary excretion of aminoimidazolecarboxamide in the Lesch-Nyhan syndrome.

Pediatrics. 1970 Oct;46(4):508-12.

Biochemical and genetic studies of an X-linked neurological disease (The Lesch-Nyhan syndrome).一种X连锁神经系统疾病（莱施-奈恩综合征）的生化与遗传学研究

Harvey Lect. 1971;65:175-92.

[Lesh-Nyhan syndrome. A congenital defect of purine metabolism with the clinical symptoms of gout and central nervous disorders].[莱施-奈恩综合征。一种嘌呤代谢的先天性缺陷，伴有痛风和中枢神经系统紊乱的临床症状]

Dtsch Med Wochenschr. 1970 May 8;95(19):1077-80.

Lesch-Nyhan syndrome.莱施-奈恩综合征

Paediatr Univ Tokyo. 1970 Dec;18:25-31.

[From Lesch-Nyhan disease to primary gout].[从莱施-奈恩病到原发性痛风]

Rev Eur Etud Clin Biol. 1970 Jun-Jul;15(6):605-9.

[Hyperuricemia and gout in childhood (Lesch-Nyhan syndrome)].

Med Klin. 1971 Apr 23;66(17):626-30.

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Plasma uric acid levels in children.儿童血浆尿酸水平。

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Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation.患有莱施-奈恩突变杂合子的女性外周血淋巴细胞群体的镶嵌现象。

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Hypoxanthine-guanine phosphoribosyl transferase deficiency.次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶缺乏症

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